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MEGAVISION CPX, MEGAVISION FA, MODEL I AND II

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K002920
510(k) Type
Traditional
Applicant
ESCALON MEDICAL CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/18/2000
Days to Decision
90 days
Submission Type
Summary

MEGAVISION CPX, MEGAVISION FA, MODEL I AND II

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K002920
510(k) Type
Traditional
Applicant
ESCALON MEDICAL CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/18/2000
Days to Decision
90 days
Submission Type
Summary